Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5010528 0.827 0.240 6 31273255 intron variant A/G snv 0.15 9
rs929596 0.925 0.040 2 233765830 intron variant A/G snv 0.32 9
rs1015164 0.925 3 46410189 intron variant A/C;G;T snv 8
rs535915558 0.827 0.120 12 55958494 missense variant C/T snv 2.0E-05 6
rs40837 0.925 0.120 16 28499524 3 prime UTR variant A/G snv 0.43 5
rs56061981 0.851 0.120 4 76023632 intron variant C/T snv 7.6E-02 5
rs10178992 2 233749231 intron variant T/A snv 0.37 4
rs10179091 2 233749337 intron variant T/C snv 0.49 4
rs10929301 2 233755003 splice region variant C/G;T snv 0.48 4
rs10929302 2 233757136 intron variant G/A snv 0.30 4
rs11673726 2 233755414 non coding transcript exon variant G/A;T snv 4
rs11888459 2 233747994 non coding transcript exon variant T/C snv 0.37 4
rs12662869 0.925 0.120 6 25784253 intron variant C/A snv 0.34 4
rs17862875 2 233740656 intron variant G/A snv 0.30 4
rs4148324 2 233764076 intron variant T/A;G snv 0.36 4
rs4842407 0.882 0.200 12 78807293 intron variant A/G snv 0.35 4
rs6714634 2 233756119 non coding transcript exon variant T/C snv 0.30 4
rs7604115 2 233749470 intron variant C/T snv 0.37 4
rs11012476 0.925 0.120 10 21003994 intron variant C/T snv 3.5E-02 3
rs11695484 2 233745803 intron variant A/G snv 0.30 3
rs17864701 2 233744071 intron variant C/T snv 0.30 3
rs201565523 0.925 0.240 2 218390027 missense variant C/T snv 2.9E-04 7.7E-05 3
rs2227513 1.000 0.080 12 68253559 intron variant T/C snv 0.15 3
rs2255301
CD4
0.925 0.160 12 6800276 intron variant T/C snv 0.59 0.61 3
rs3771341 2 233764593 intron variant G/A;T snv 0.33 3